Stephanie received her professional Master's of Science in Clinical Pharmacology with an emphasis in Clinical Trial Design from the Ohio State University. Before joining Proxima, she worked in clinical trial development, trial management, medical writing, and as a consultant to investigator-sponsors. She has extensive oncology experience, including solid tumors and hematological malignancies and dyscrasias.
Stephanie helps clients develop and write essential documents, such as clinical trial protocols, investigator brochures, and clinical study reports, appropriate for their phase of development and regulatory strategy.
Stephanie loves the outdoors and will take almost any excuse (e.g., cycling, running, camping, hiking, etc.) to go outside to play.